Abstract 1417P
Background
Tislelizumab has demonstrated survival benefit over chemotherapy in previously treated advanced esophageal squamous cell carcinoma (ESCC) in an open-label phase 3 study (RATIONALE 302, N=512, NCT03430843). In the absence of head-to-head studies, anchored simulated treatment comparisons (STCs) estimated the relative effect of tislelizumab versus other anti-PD-1 treatments approved in the European Union and United Kingdom.
Methods
Individual patient data from RATIONALE 302 were adjusted to aggregate data in each comparator study using STC. Clinical expert input, statistical analyses and literature searches determined important effect modifiers. Depending on data availability, STCs for overall survival (OS) and progression-free survival (PFS) were adjusted for Eastern Cooperative Oncology Group performance status (ECOG-PS), disease status, PD-1 expression status, liver and lung metastasis; whereas STC for treatment-related adverse event (TRAE) grade ≥ 3 analysis was adjusted for age, ECOG-PS, PD-1 expression, liver metastasis, and previous therapies. Additional sensitivity analyses along with subgroup analyses (PD-1 category and baseline ECOG-PS) were considered. These analyses were also conducted using the latest DCO (Dec 28, 2022).
Results
Comparator studies were similar to RATIONALE 302 with comparable control arms. After adjustment, no significant differences were estimated in PFS, OS, or TRAEs between tislelizumab and anti-PD-1 comparators (Table). Results from sensitivity, subgroup and latest DCO aligned with the base case. Table: 1417P
Population-adjusted relative effects in the base case
Tislelizumab (RATIONALE 302) versus comparator (study) | OS | PFS | TRAE grade ≥3 |
HR (95% CI) | HR (95% CI) | OR (95% CI) | |
Nivolumab (ATTRACTION-3) | 0.88 (0.65, 1.19) | 0.79 (0.59, 1.07) | 1.30 (0.68, 2.48) |
Pembrolizumab (KEYNOTE-181) | 0.94 (0.67, 1.32) | 0.95 (0.63, 1.43) | Not feasible* |
CI, Confidence Interval; HR, Hazard ratio; OR, Odds ratio. *TRAE data was not available for pembrolizumab. DCO=Dec 01, 2020
Conclusions
The STCs showed comparable efficacy and safety between tislelizumab, pembrolizumab, and nivolumab.
Clinical trial identification
NCT03430843.
Editorial acknowledgement
Editorial support, under the direction of the authors, was provided by Smitha Reddy, PhD, of Envision Pharma Inc.
Legal entity responsible for the study
BeiGene, Ltd.
Funding
BeiGene, Ltd.
Disclosure
E.C. Smyth: Financial Interests, Personal, Invited Speaker: Amgen, Bristol Myers Squibb, Imedex, Merck, Novartis, Prova Education, Servier, TouchIME, Elsevier, Peervoice, Cor2Ed, Daiichi Sankyo, MSD, Suzhou Liangihui Network Technology Company Ltd. Financial Interests, Personal, Other, TSC: Amgen; Financial Interests, Personal, Advisory Board: Astellas, AstraZeneca, Bristol Myers Squibb, Bristol Myers Squibb, My Personal Therapeutics, Novartis, Roche, Servier, Zymeworks, Viracta, Boehringer Ingelheim, AbbVie, Natera; Financial Interests, Personal, Other, IDMC: BeiGene, Zymeworks; Financial Interests, Personal, Other, IDMC chair: Everest Clinical Research; Financial Interests, Personal, Other, IDMC Chair: Jazz Pharmaceuticals; Financial Interests, Personal, Officer: EORTC GI Clinical Trials Group; Financial Interests, Institutional, Local PI: Daiichi Sankyo, Merus, Basilea, MSD, Mirati; Financial Interests, Institutional, Coordinating PI: Roche, AstraZeneca, Amgen; Financial Interests, Institutional, Research Grant: Bristol Myers Squibb, AstraZeneca; Non-Financial Interests, Leadership Role, Trustee: UK & Ireland Oesophagogastric Group (UKIOG). J.A. Ajani: Financial Interests, Personal, Advisory Board: BMS, Gilead, Astellas, AZ, Jazz, KirinKyowa, Servier, BeiGene, Daiichi Sankyo; Financial Interests, Institutional, Coordinating PI, My institution receives funding: BMS; Financial Interests, Institutional, Coordinating PI: Merck, Jazz, Astellas, Delta Fly, Gilead, Roche. K. Wang: Financial Interests, Personal, Full or part-time Employment: BeiGene; Financial Interests, Personal, Stocks or ownership: BeiGene. J. Coaquira Castro: Financial Interests, Personal, Other, Travel: BeiGene; Financial Interests, Personal, Stocks or ownership: BeiGene, Jazz Pharmaceuticals. M. Figueiredo: Financial Interests, Personal, Speaker, Consultant, Advisor: Pfizer; Financial Interests, Personal, Invited Speaker: Pfizer. K. Soulanis, A. Tasoulas, G. Nikolaidis: Financial Interests, Personal, Full or part-time Employment: IQVIA. E. Priedane: Financial Interests, Personal, Full or part-time Employment: BeiGene. L. Zhan: Financial Interests, Personal, Full or part-time Employment: BeiGene; Financial Interests, Personal, Stocks or ownership: BeiGene; Financial Interests, Personal, Other, Travel: BeiGene. All other authors have declared no conflicts of interest.
Resources from the same session
498P - Report of 9 cases of embryonal tumours of the central nervous system with multilayered rosettes (ETMR)
Presenter: Ruyu Ai
Session: Poster session 17
Resources:
Abstract
499TiP - A phase II study of BPM31510 (a lipid nanodispersion of oxidized CoQ10) with vitamin K in combination with standard of care (SOC) RT and TMZ in glioblastoma multiforme (GBM) patients without prior therapy
Presenter: Brian Stockdale
Session: Poster session 17
500TiP - Update on GBM AGILE: A global, phase II/III adaptive platform trial to evaluate multiple regimens in newly diagnosed and recurrent glioblastoma
Presenter: Michael Weller
Session: Poster session 17
501TiP - Clinical performance evaluation of a brain cancer liquid biopsy
Presenter: James Cameron
Session: Poster session 17
692P - Role of adjunctive surgery after platinum-based chemotherapy in management patients with adrenocortical carcinoma: Observation study
Presenter: Yaroslav Zhulikov
Session: Poster session 17
693P - Causes of death in patients with malignant adrenal tumors: A population-based analysis
Presenter: Shangqing Ren
Session: Poster session 17
946P - Ipilimumab and nivolumab in advanced hepatocellular carcinoma after failure of prior atezolizumab and bevacizumab treatment: A multicenter retrospective study
Presenter: Jung Sun Kim
Session: Poster session 17
948P - Drug type and duration of adjuvant immune checkpoint inhibitors in hepatocellular carcinoma with high-risk recurrence factors (PREVENT): An update analysis of a prospective, multicentric cohort study
Presenter: Jia-Yong Su
Session: Poster session 17
Resources:
Abstract
949P - Update results of ALTER-H006: A phase II study of TQB2450 plus anlotinib as adjuvant therapy in hepatocellular carcinoma (HCC) with high risk of recurrence after surgical resection
Presenter: Xianhai Mao
Session: Poster session 17
950P - Outcomes by baseline tumour burden in EMERALD-1: A phase III, randomised, placebo (PBO)-controlled study of durvalumab (D) ± bevacizumab (B) with transarterial chemoembolisation (TACE) in participants (pts) with embolisation-eligible unresectable hepatocellular carcinoma (uHCC)
Presenter: Masatoshi Kudo
Session: Poster session 17